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6-Quinolineacetic acid, 1,2,3,4-tetrahydro-, methyl ester is a chemical compound with the molecular formula C12H15NO2. It is a derivative of quinolineacetic acid, featuring a methyl ester group attached to the carboxylic acid functionality. 6-Quinolineacetic acid, 1,2,3,4-tetrahydro-, methyl ester is a part of the quinoline family, which is a group of heterocyclic compounds with a benzene ring fused to a pyridine ring. The 1,2,3,4-tetrahydro prefix indicates that the compound has undergone hydrogenation, resulting in a saturated ring structure. The methyl ester group provides the compound with ester-like properties, which can influence its reactivity and solubility. 6-Quinolineacetic acid, 1,2,3,4-tetrahydro-, methyl ester has potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties.

5622-50-4

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5622-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5622-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5622-50:
(6*5)+(5*6)+(4*2)+(3*2)+(2*5)+(1*0)=84
84 % 10 = 4
So 5622-50-4 is a valid CAS Registry Number.

5622-50-4Downstream Products

5622-50-4Relevant articles and documents

Discovery of IDO1 inhibitors containing a decahydroquinoline, decahydro-1,6-naphthyridine, or octahydro-1H-pyrrolo[3,2-c]pyridine scaffold

Deng, Yongqi,Doty, Amy,Ferguson, Heidi,Fradera, Xavier,Han, Yongxin,Jonathan Bennett, David,Knemeyer, Ian,Lesburg, Charles A.,Li, Derun,Liu, Kun,Martinot, Theo,Otte, Karin,Richard Miller, J.,Sciammetta, Nunzio,Sloman, David,Vincent, Stella,Yu, Wensheng

, (2021/08/27)

A series of IDO1 inhibitors containing a decahydroquinoline, decahydro-1,6-naphthyridine, or octahydro-1H-pyrrolo[3,2-c]pyridine scaffold were identified with good cellular and human whole blood activity against IDO1. These inhibitors contain multiple chiral centers and all diastereomers were separated. The absolute stereochemistry of each isomers were not determined. Compounds 15 and 27 stood out as leads due to their good cellular as well as human whole blood IDO1 inhibition activity, low unbound clearance, and reasonable mean residence time in rat cassette PK studies.

NOVEL SUBSTITUTED TETRAHYDROQUINOLIN COMPOUNDS AS INDOLEAMINE 2,3-DIOXYGENASE (IDO) INHIBITORS

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Page/Page column 42; 43, (2020/12/30)

Disclosed herein is a compound of formula (I), or a pharmaceutically acceptable salt thereof: Also disclosed herein are uses of the compounds disclosed herein in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclose

NOVEL SUBSTITUTED TETRAHYDROQUINOLIN COMPOUNDS AS INDOLEAMINE 2,3-DIOXYGENASE (IDO) INHIBITORS

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Page/Page column 77, (2019/05/22)

Disclosed herein is a compound of formula (I), or a pharmaceutically acceptable salt thereof (I). Also disclosed herein are uses of the compounds disclosed herein in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising a compound disclosed herein. Further disclosed herein are uses of the compositions in the potential treatment or prevention of an IDO-associated disease or disorder.

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